CRO Contract Research Organization Nantes

Our jobs

Medical writing

Our medical writers produce pre-clinical and clinical study reports, publications or any other medical document in compliance with the regulations, in particular ICH, in English or French.
They can also prepare numerous clinical regulatory documents from the initiation of the study to the final report.

Clinical operations

The experience acquired by the ATLANSTAT team in the drafting of protocols, submissions and obtaining regulatory authorisations guarantees a controlled start of the studies. The monitoring allows to keep this quality requirement.

Randomization

A crucial step in a trial, randomisation allows to avoid selection bias, to ensure comparability between the different groups and to legitimise the use of statistical tests. ATLANSTAT has a proven statistical methodological expertise as well as an operational know-how in the implementation of IWRS (Interactive Web Response System).

Data Management

ATLANSTAT masters the clinical data management process in compliance with international recommendations (EMA, ICH, FDA). It allows the complete management of the data of a study, from the elaboration of the CRF with the help of the protocol to the final database, validated, for a statistical analysis of quality.

Biostatistics

With a highly qualified biostatisticians and statistical programmers team, we are regularly asked to define statistical methodology, write protocols, produce and interpret statistical results or participate in DSMBs (Data Safety Monitoring Board)

Our team

Qualified and experienced

The team of our Contrat Research Organization ATLANSTAT shares the same passion for clinical development in a climate of trust and collaboration, listening to both its clients and colleagues.

Examples of Case studies

Here are a few examples of case studies our Contrat Research Organization carried out on an internal or contract basis, for any type of therapeutic area. This list is not exhaustive and all requests are studied.

CE marking

Obtaining CE marking for a medical device

E-CRF

Design of an e-CRF

Clinical study

Complete set-up and management of a clinical study

IWRS

Setting up an online randomization tool (IWRS)

Monitoring

Managing the monitoring of a clinical study

Programming the results

Programming the results of a clinical study (Tables, Listings, Figures) from an ADaM database

CRO in clinical research and development : a multi-skilled partner